Zaniboni A, Formica V
Medical Oncology Dept, Fondazione Poliambulanza, Via Bissolati 57, 25124, Brescia, Italy.
Medical Oncology Unit, Tor Vergata University Hospital, Rome, Italy.
Cancer Chemother Pharmacol. 2016 Aug;78(2):233-44. doi: 10.1007/s00280-016-3032-8. Epub 2016 Apr 18.
Since 2013, informative trials exploring the optimal use of available biologic agents in the first-line setting of metastatic colorectal cancer (mCRC) have been presented. These trials have opened a stimulating debate on the biological effect that first-line therapies may have on subsequent lines of treatment even long after the first-line progression.
We reviewed available preclinical and clinical data on the effect of different sequences of the biological drugs approved for use in mCRC patients. The importance of molecular selection of patients based on RAS mutational status and toxicity and quality-of-life issues were also analyzed.
Convincing evidence exists on the optimal therapeutic effect obtained by using anti-EGFR agents in first-line treatment before anti-VEGF agents. On the contrary, up-front anti-VEGF agents' use seems to determine biological changes that increase the risk of acquired resistance to subsequent EGFR inhibitors. This hypothesis is confirmed by the scarce evidence of EGFR inhibitor activity in second-line treatment. Such a therapeutic optimum is subject to a fine molecular selection based on RAS mutational status.
There is accumulating evidence suggesting that, after precise and well-established molecular selection, anti-EGFR agents deliver their maximum efficacy in mCRC patients when given early in the treatment strategy. Their toxicity profile seems manageable under the supervision of experienced physicians. Large randomized trials prospectively confirming the impact of different sequencing strategies are eagerly awaited.
自2013年以来,已有多项探索在转移性结直肠癌(mCRC)一线治疗中最佳使用现有生物制剂的信息性试验。这些试验引发了一场激烈的辩论,即一线治疗对后续治疗线可能产生的生物学效应,即使在一线治疗进展很久之后。
我们回顾了关于批准用于mCRC患者的生物药物不同用药顺序效果的现有临床前和临床数据。还分析了基于RAS突变状态进行患者分子选择的重要性以及毒性和生活质量问题。
有令人信服的证据表明,在一线治疗中先使用抗EGFR药物再使用抗VEGF药物可获得最佳治疗效果。相反, upfront使用抗VEGF药物似乎会导致生物学变化,增加后续对EGFR抑制剂获得性耐药的风险。二线治疗中EGFR抑制剂活性的证据稀少证实了这一假设。这种治疗最佳方案需要基于RAS突变状态进行精细的分子选择。
越来越多的证据表明,在经过精确且成熟的分子选择后,抗EGFR药物在治疗策略早期给予mCRC患者时可发挥最大疗效。在经验丰富的医生监督下,其毒性似乎可控。迫切期待大型前瞻性随机试验来证实不同用药顺序策略的影响。